Provide guidance, lead/co-lead projects, manage own time to meet objectives, plan resource requirements for projects across the Department. Contribute to Quality Assurance by undertaking a variety of roles or assignments to further develop internal processes and people. Assess the operations executed at the supplier for their adherence to regulatory requirements, Quality Agreement requirements and *** expectations. Conduct quality reviews and report on results or defined quality analytics to in-country Medical Management, Platform Lines and Regional Medical Quality group, as appropriate.
Provides project support with current Good Manufacturing Practices to clinical supply packaging operations. Provides guidance on procedures and training necessary to be in complete compliance with current GMPs.
Intake Notes:
Hard Skills:
Plus Skill:
BS Preferred
(open to 5 + years’ experience in lieu of degree)
Hybrid: Required Onsite 2-3 days per weeks, will need to be local to the Groton Site.
Interview Process:
Strictly GMPs for this role, not GCP
Hybrid: Required Onsite 2-3 days per weeks, will need to be local to the Groton Site.
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